FDA inspection
Linvatec Biomaterials, Inc.: FDA inspection ending Oct 29, 1999
FDA inspection 4609 · Voluntary Action Indicated (VAI) · Blue Bell, PA
Key facts
| Inspection ID | 4609 |
|---|---|
| Firm | Linvatec Biomaterials, Inc. |
| FEI number | 1000522769 |
| Address | 1777 Sentry Pkwy West, Gwyned Hall, Suite 400 |
| City | Blue Bell |
| State | PA |
| ZIP | 19422 |
| Fiscal year | 2000 |
| Inspection end date | Oct 29, 1999 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data